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    NDC 57896-0619-12 GERI-LANTA MAXIMUM STRENGTH 400; 40; 400 mg/5mL; mg/5mL; mg/5mL Details

    GERI-LANTA MAXIMUM STRENGTH 400; 40; 400 mg/5mL; mg/5mL; mg/5mL

    GERI-LANTA MAXIMUM STRENGTH is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by Geri-Care Pharmaceuticals, Corp. The primary component is ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE.

    Product Information

    NDC 57896-0619
    Product ID 57896-619_09a8019b-b747-463f-e063-6394a90af5d0
    Associated GPIs 48991003101835
    GCN Sequence Number 002706
    GCN Sequence Number Description mag hydrox/aluminum hyd/simeth ORAL SUSP 400-400-40 ORAL
    HIC3 D4B
    HIC3 Description ANTACIDS
    GCN 63915
    HICL Sequence Number 001168
    HICL Sequence Number Description MAGNESIUM HYDROXIDE/ALUMINUM HYDROXIDE/SIMETHICONE
    Brand/Generic Generic
    Proprietary Name GERI-LANTA MAXIMUM STRENGTH
    Proprietary Name Suffix n/a
    Non-Proprietary Name aluminum hydroxide, magnesium hydroxide, dimethicone
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 400; 40; 400
    Active Ingredient Units mg/5mL; mg/5mL; mg/5mL
    Substance Name ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE
    Labeler Name Geri-Care Pharmaceuticals, Corp
    Pharmaceutical Class Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M001
    Listing Certified Through 2024-12-31

    Package

    NDC 57896-0619-12 (57896061912)

    NDC Package Code 57896-619-12
    Billing NDC 57896061912
    Package 355 mL in 1 BOTTLE (57896-619-12)
    Marketing Start Date 2011-01-01
    NDC Exclude Flag N
    Pricing Information N/A